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Journal Abstract Search

436 related items for PubMed ID: 19074151

  • 1. Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection.
    Hizume M, Kobayashi A, Teruya K, Ohashi H, Ironside JW, Mohri S, Kitamoto T.
    J Biol Chem; 2009 Feb 06; 284(6):3603-9. PubMed ID: 19074151
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  • 2. Heterozygous inhibition in prion infection: the stone fence model.
    Kobayashi A, Hizume M, Teruya K, Mohri S, Kitamoto T.
    Prion; 2009 Feb 06; 3(1):27-30. PubMed ID: 19372732
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  • 3. A traceback phenomenon can reveal the origin of prion infection.
    Kobayashi A, Asano M, Mohri S, Kitamoto T.
    Neuropathology; 2009 Oct 06; 29(5):619-24. PubMed ID: 19659941
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  • 4. A naturally occurring variant of the human prion protein completely prevents prion disease.
    Asante EA, Smidak M, Grimshaw A, Houghton R, Tomlinson A, Jeelani A, Jakubcova T, Hamdan S, Richard-Londt A, Linehan JM, Brandner S, Alpers M, Whitfield J, Mead S, Wadsworth JD, Collinge J.
    Nature; 2015 Jun 25; 522(7557):478-81. PubMed ID: 26061765
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  • 7. Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.
    Takeuchi A, Kobayashi A, Ironside JW, Mohri S, Kitamoto T.
    J Biol Chem; 2013 Jul 26; 288(30):21659-66. PubMed ID: 23792955
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  • 8. Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay.
    Jones M, Peden AH, Wight D, Prowse C, Macgregor I, Manson J, Turner M, Ironside JW, Head MW.
    Neuroreport; 2008 Dec 03; 19(18):1783-6. PubMed ID: 18955905
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  • 17. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
    Bishop MT, Pennington C, Heath CA, Will RG, Knight RS.
    BMC Med Genet; 2009 Dec 26; 10():146. PubMed ID: 20035629
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